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As one of the most experienced staffing firms in Denver Colorado, North Star Staffing Solutions prides itself on exceptional services and relationships we've built over the years. We have continued to provide the recruiting and staffing expertise our clients expect and they have acknowledged over and over again that our services are integral to their success.
• Supervise multi-skilled personnel as assigned, to ensure that performance meets established safety, quality/Good Manufacturing Practices (cGMP), quantity and cost standards.
• Manage, coordinate and directly supervise employees including coaching, counseling, performance reviews and feedback/initiating corrective action as needed, in a timely fashion.
• Collaborate with other area supervision and Human Resources in ensuring consistency in situations requiring corrective action with employees.
• Provide leadership and support to production and non-exempt production personnel in solving technical problems or contacting other resources as appropriate to solve problems.
• Ensure compliance of local, state and federal regulations and guidelines (e.g., Good Manufacturing Practices (CGMP), Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), etc.). Ensure SOPs for areas of responsibility are updated, accurate, and complete.
• Ensure formal and informal training occurs in employee technical skill development as well as other training initiatives including safety, CGMP, teamwork, etc.
• Support the Head of Manufacturing in the timely completion of assigned projects, including participating in the design and development of new packaging/production materials, equipment and packages.
• Participate in cost reduction programs with respect to waste and other inefficiencies.
• Perform other supervision duties and responsibilities as assigned
-Bachelor’s degree and at least 4 years production supervisory experience in a government regulated industry using QA procedures (FDA, pharmaceutical industry preferred).
-If no degree, but have 5 years’ supervisory/leadership GMP packaging/liquids experience, must commit to start/continue college degree / certification program.
-Master''s degree & 2 years’ experience listed above or PhD and 1 year experience listed above may be considered.
-Strong personal computer skills required experience with windows environment, Microsoft WORD and Excel preferred. Knowledge of automated Materials Requirement Planning (i.e. MES) system preferred.
-Demonstrated ability to communicate positively with personnel at all levels.
All your information will be kept confidential according to EEO guidelines
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